Richter Matthias H, Lublow Michael, Papadantonakis Kimberly M, Lewis Nathan S, Lewerenz Hans-Joachim
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Technische Universität Berlin, Institut für Chemie, Straße des 17. Juni 124, 10623 Berlin, Germany.
ACS Appl Mater Interfaces. 2020 Apr 8;12(14):17018-17028. doi: 10.1021/acsami.9b22900. Epub 2020 Mar 30.
The genesis, propagation, and dimensions of fractal-etch patterns that form anodically on front- or back-illuminated n-Si(100) photoelectrodes in contact with 11.9 M NHF (aqueous) have been investigated during either a linear potential sweep or a constant potential hold ( = +6.0 V versus Ag/AgCl). Optical images collected in situ during electrochemical experiments revealed the location and underlying mechanism of initiation and propagation of the structures on the surface. X-ray photoelectron spectroscopic (XPS) data collected for samples emersed from the electrolyte at varied times provided detailed information about the chemistry of the surface during fractal etching. The fractal structure was strongly influenced by the orientation of the crystalline Si sample. The etch patterns were initially generated at points along the circumference of bubbles that formed upon immersion of n-Si(100) samples in the electrolyte, most likely due to the electrochemical and electronic isolation of areas beneath bubbles. XPS data showed the presence of a tensile-stressed silicon surface throughout the etching process as well as the presence of SiOF on the surface. The two-dimensional fractal dimension, , of the patterns increased with etching time to a maximum observed value of = 1.82. Promotion of fractal etching near etch masks that electrochemically and electronically isolated areas of the photoelectrode surface enabled the selective placement of highly branched structures at desired locations on an electrode surface.
在与11.9 M NHF(水溶液)接触的正面或背面照明的n-Si(100)光电极上,通过线性电位扫描或恒电位保持(相对于Ag/AgCl为+6.0 V),研究了阳极形成的分形蚀刻图案的起源、传播和尺寸。在电化学实验过程中现场收集的光学图像揭示了表面结构起始和传播的位置及潜在机制。对在不同时间从电解液中取出的样品收集的X射线光电子能谱(XPS)数据提供了有关分形蚀刻过程中表面化学的详细信息。分形结构受到晶体硅样品取向的强烈影响。蚀刻图案最初在n-Si(100)样品浸入电解液时形成的气泡圆周上的点处产生,这很可能是由于气泡下方区域发生了电化学和电子隔离。XPS数据表明在整个蚀刻过程中存在拉伸应力的硅表面以及表面上存在SiOF。图案的二维分形维数D随蚀刻时间增加,达到最大值D = 1.82。在电化学和电子隔离光电极表面区域的蚀刻掩膜附近促进分形蚀刻,能够在电极表面的所需位置选择性地放置高度分支的结构。